Rusch V, Saltz L, Venkatraman E, Ginsberg R, McCormack P, Burt M, Markman M, Kelsen D
Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY 10021.
J Clin Oncol. 1994 Jun;12(6):1156-63. doi: 10.1200/JCO.1994.12.6.1156.
This study investigated the feasibility of a novel approach to the treatment of malignant pleural mesothelioma by combining surgical resection with immediate postoperative intrapleural chemotherapy and subsequent systemic chemotherapy.
Patients with biopsy-proven, resectable malignant pleural mesothelioma underwent pleurectomy/decortication immediately followed by intrapleural chemotherapy with cisplatin 100 mg/m2 and mitomycin 8 mg/m2. Systemic chemotherapy was started 3 to 5 weeks postoperatively and included cisplatin 50 mg/m2 on days 1, 8, 15, 22, 36, 43, 50, and 57, and mitomycin 8 mg/m2 on days 1 and 36. Patients were then monitored by serial chest and abdominal computed tomographic (CT) scans every 3 months until death or for a minimum of 18 months, whichever occurred first.
Of 36 patients entered onto the study, 28 had pleurectomy/decortication and intrapleural chemotherapy. There was one postoperative death, and two episodes of grade 4 renal toxicity after intrapleural chemotherapy. The 23 patients who also had systemic chemotherapy received a median of 80% and 87% of the planned total cisplatin and mitomycin doses, respectively. No grade 3 or 4 toxicities were observed. The overall survival rate of the 27 patients who were originally candidates for systemic chemotherapy was 68% at 1 year and 40% at 2 years, with a median survival duration of 17 months. Locoregional disease was the most common form of relapse (16 of 20 patients).
This short but aggressive combined modality regimen was generally well tolerated, but should not be used outside of a protocol setting because of the potential for serious toxicity. Overall survival was as good or better than with previously reported multimodality approaches, but other strategies are needed to improve local control.
本研究探讨了一种新的治疗恶性胸膜间皮瘤的方法,即手术切除联合术后即刻胸膜腔内化疗及后续全身化疗的可行性。
经活检证实为可切除的恶性胸膜间皮瘤患者接受胸膜剥脱术/去皮质术,随后立即进行胸膜腔内化疗,顺铂剂量为100mg/m²,丝裂霉素剂量为8mg/m²。全身化疗在术后3至5周开始,包括顺铂50mg/m²,分别在第1、8、15、22、36、43、50和57天给药,丝裂霉素8mg/m²,分别在第1天和第36天给药。然后每3个月对患者进行胸部和腹部计算机断层扫描(CT)连续监测,直至死亡或至少18个月,以先发生者为准。
36例纳入研究的患者中,28例接受了胸膜剥脱术/去皮质术及胸膜腔内化疗。术后有1例死亡,胸膜腔内化疗后有2例发生4级肾毒性。23例接受全身化疗的患者分别接受了计划总顺铂和丝裂霉素剂量的中位数80%和87%。未观察到3级或4级毒性反应。最初适合进行全身化疗的27例患者的1年总生存率为68%﹒2年总生存率为40%,中位生存时间为17个月。局部区域疾病是最常见的复发形式(20例患者中有16例)。
这种短疗程但积极的联合治疗方案总体耐受性良好,但由于存在严重毒性的可能性,不应在非方案设定的情况下使用。总体生存率与先前报道的多模式治疗方法相当或更好,但需要其他策略来改善局部控制。